Control nucleic acid sequences for use in sequencing-by-synthesis and methods for designing the same

ABSTRACT

A method for nucleic acid sequencing includes (a) disposing a plurality of template polynucleotide strands in a plurality of defined spaces disposed on a sensor array, at least some of the template polynucleotide strands comprising a test or control sequence; (b) exposing a plurality of the template polynucleotide strands in the defined spaces to a series of flows of nucleotide species flowed according to a predetermined ordering; and (c) determining sequence information for a plurality of the template polynucleotide strands in the defined spaces based on the flows of nucleotide species to generate a plurality of sequencing reads corresponding to the template polynucleotide strands, wherein the test or control sequence comprises a sequence determined by identifying, using a variant caller, loci with systematic errors present in a plurality of sequencing runs included in a training set of sequencing runs.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Prov. Pat. Appl. No. 61/858,828, filed Jul. 26, 2013, which is incorporated by reference herein in its entirety.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Oct. 5, 2014, is named LT00835_ST25.txt and is 22,430 bytes in size.

FIELD

This application generally relates to control nucleic acid sequences and methods for designing the same, and, more specifically, to control nucleic acid sequences for use in sequencing-by-synthesis and methods for designing the same using a variant caller to identify loci with systematic errors.

BACKGROUND

Control nucleic acid sequences may sometimes be used to facilitate assessment and/or analysis of nucleic acid sequencing data obtained in various ways, including using next-generation sequencing systems such as, for example, the Ion PGM™ and Ion Proton™ systems implementing Ion Torrent™ sequencing technology (see, e.g., U.S. Pat. No. 7,948,015 and U.S. Pat. Appl. Publ. Nos. 2010/0137143, 2009/0026082, and 2010/0282617, which are all incorporated by reference herein in their entirety). For example, certain relatively short (e.g., less than 100 base pairs) nucleic acid sequences constrained to contain homopolymers of only certain lengths (e.g., homopolymers of length two, three, or four; homopolymers of length no more than 2; or homopolymers of length no more than 1) may be used to attempt to assess potential error failure modes that may be related to homopolymer of such lengths and may more generally be indicative of performance. However, these nucleic acid sequences may in some cases be oversensitive and may not be able to properly capture or detect certain error modes of interest. There is a need for new and improved control nucleic acid sequences and methods for designing the same that can better facilitate assessment and/or analysis of nucleic acid sequencing data obtained using the above-mentioned systems or other sequencing systems/platforms.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated into and form a part of the specification, illustrate one or more exemplary embodiments and serve to explain the principles of various exemplary embodiments. The drawings are exemplary and explanatory only and are not to be construed as limiting or restrictive in any way.

FIG. 1 illustrates an exemplary system for nucleic acid sequencing and/or analysis.

FIG. 2 illustrates exemplary components of an apparatus for nucleic acid sequencing.

FIG. 3 illustrates an exemplary flow cell for nucleic acid sequencing.

FIG. 4 illustrates an exemplary process for label-free, pH-based sequencing.

FIG. 5 illustrates an exemplary computer system.

FIG. 6 illustrates an exemplary method for nucleic acid sequencing using control sequences.

FIG. 7 illustrates an exemplary method for generating control sequences.

FIG. 8 illustrates an exemplary method for generating control sequences.

FIGS. 9A and 9B show plots of unique variants according to nucleotide and homopolymer length.

SUMMARY

According to an exemplary embodiment, there is provided a method for nucleic acid sequencing, comprising: (a) disposing a plurality of template polynucleotide strands in a plurality of defined spaces disposed on a sensor array, at least some of the template polynucleotide strands comprising a test or control sequence; (b) exposing a plurality of the template polynucleotide strands in the defined spaces to a series of flows of nucleotide species flowed according to a predetermined ordering; and (c) determining sequence information for a plurality of the template polynucleotide strands in the defined spaces based on the flows of nucleotide species to generate a plurality of sequencing reads corresponding to the template polynucleotide strands, wherein the test or control sequence comprises a sequence determined by identifying, using a variant caller, loci with systematic errors present in a plurality of sequencing runs included in a training set of sequencing runs.

According to an exemplary embodiment, there is provided a system, including: a plurality of template polynucleotide strands disposed in a plurality of defined spaces disposed on a sensor array, at least some of the template polynucleotide strands comprising a test or control sequence, wherein the test or control sequence comprises a sequence determined by identifying, using a variant caller, loci with systematic errors present in a plurality of sequencing runs included in a training set of sequencing runs; a machine-readable memory; and a processor configured to execute machine-readable instructions, which, when executed by the processor, cause the system to perform a method for nucleic acid sequencing, comprising: (a) exposing a plurality of the template polynucleotide strands in the defined spaces to a series of flows of nucleotide species flowed according to a predetermined ordering; and (b) determining sequence information for a plurality of the template polynucleotide strands in the defined spaces based on the flows of nucleotide species to generate a plurality of sequencing reads corresponding to the template polynucleotide strands.

According to an exemplary embodiment, there is provided a method for designing test or control sequences, comprising: identifying, using a variant caller, loci with systematic errors present in a plurality of sequencing runs included in a training set of sequencing runs obtained using sequencing-by-synthesis; selecting a representative set of loci, including selecting from the identified loci an approximately equal number of loci involving errors in A, T, C, and G homopolymers and selecting from the identified loci an approximately equal number of loci involving homopolymers having a length of two, three, and four.

Exemplary Embodiments

The following description and the various embodiments described herein are exemplary and explanatory only and are not to be construed as limiting or restrictive in any way. Other embodiments, features, objects, and advantages of the present teachings will be apparent from the description and accompanying drawings, and from the claims.

According to various exemplary embodiments, control nucleic acid sequences for test fragments and/or in line controls, and methods for designing the same, are disclosed herein. Such control nucleic acid sequences and methods for designing the same may improve the ability of control nucleic acid sequences to allow identification of compromised sequencing experiments that produce data of substandard quality as a result of sequencing failure modes. Such sequencing failure modes may include sequencing failure modes that lead to reduced accuracy, which may include one or more sequencing failure modes such as: systematic errors for high homopolymers in general, systematic errors for high homopolymers in specific contexts, and/or systematic errors for specific “difficult” sequences not involving high homopolymers. Such control nucleic acid sequences and methods for designing the same may help detect and/or reduce certain systematic errors and improve overall sequencing accuracy (especially in the case of long homopolymers), which may in turn improve downstream processing such as variant calling.

FIG. 1 illustrates an exemplary system for nucleic acid sequencing and/or analysis. The system includes an apparatus or sub-system for nucleic acid sequencing and/or analysis 11, a computing server/node/device 12 including a base calling engine 13, a recalibration engine 14, a post-processing engine 15, and a display 16, which may be internal and/or external. The apparatus or sub-system for nucleic acid sequencing and/or analysis 11 may be any type of instrument that can generate nucleic acid sequence data from nucleic acid samples, which may include a nucleic acid sequencing instrument, a real-time/digital/quantitative PCR instrument, a microarray scanner, etc. The nucleic acid samples may include control/test nucleic acid samples as further described herein and/or library nucleic acid samples. The computing server/node/device 12 may be a workstation, mainframe computer, distributed computing node (part of a “cloud computing” or distributed networking system), personal computer, mobile device, etc. The base calling engine 13 may be any suitable base caller and may be configured to include various signal/data processing modules that may be configured to receive signal/data from the apparatus or sub-system for nucleic acid sequencing and/or analysis 11 and perform various processing steps, such as conversion from flow space to base space, determination of base calls for some or the entirety of a sequencing data set, and determination of base call quality values. In an embodiment, the base calling engine 13 may implement one or more features described in Davey et al., U.S. Pat. Appl. Publ. No. 2012/0109598, published on May 3, 2012, and/or Sikora et al., U.S. Pat. Appl. Publ. No. 2013/0060482, published on Mar. 7, 2013, which are all incorporated by reference herein in their entirety. The base calling engine 13 may also include a mapping or alignment module for mapping or aligning reads to a reference sequence or genome, which may be a whole/partial genome, whole/partial exome, etc. In an embodiment, the mapping or alignment module may include any suitable aligner, including the Torrent Mapping Alignment Program (TMAP), for example. The recalibration engine 14 may be configured to recalibrate base calls or related intensity values or parameters based on an analysis of base calling and alignment performed by the base calling engine 13, which recalibrated base calls or related intensity values or thresholds or parameters may be fed back into the base calling engine 13 for improving the accuracy of base calls. In an embodiment, the recalibration engine 14 may implement one or more features described in Jiang et al., U.S. patent application Ser. No. 14/255,528, filed on Apr. 17, 2014, which is incorporated by reference herein in its entirety. The exemplary system may also include a client device terminal 17, which may include a data analysis API or module and may be communicatively connected to the computing server/node/device 12 via a network connection 18 that may be a “hardwired” physical network connection (e.g., Internet, LAN, WAN, VPN, etc.) or a wireless network connection (e.g., Wi-Fi, WLAN, etc.). The post-processing engine 15 may be configured to include various signal/data processing modules that may be configured to make variant calls and apply post-processing to variant calls, which may include annotating various variant calls and/or features, converting data from flow space to base space, filtering of variants, and formatting the variant data for display or use by client device terminal 17. Variant calls may be made using any suitable variant caller, including the Germ-Line Variant Caller and the Torrent Variant Caller (TVC) Plug-ins for Ion Torrent™ sequencing technology. In an embodiment, the variant caller may implement one or more features described in Hubbell et al., U.S. patent application Ser. No. 14/200,942, filed Mar. 7, 2014, which is incorporated by reference herein in its entirety. In an embodiment, the apparatus or sub-system for nucleic acid sequencing and/or analysis 11 and the computing server/node/device 12 may be integrated into a single instrument or system comprising components present in a single enclosure 19. The client device terminal 17 may be configured to communicate information to and/or control the operation of the computing server/node/device 12 and its modules and/or operating parameters.

FIG. 2 illustrates exemplary components of an apparatus for nucleic acid sequencing. Such an apparatus could be used as apparatus or sub-system for nucleic acid sequencing and/or analysis 11 of FIG. 1. The components include a flow cell and sensor array 100, a reference electrode 108, a plurality of reagents 114, a valve block 116, a wash solution 110, a valve 112, a fluidics controller 118, lines 120/122/126, passages 104/109/111, a waste container 106, an array controller 124, and a user interface 128. The flow cell and sensor array 100 includes an inlet 102, an outlet 103, a microwell array 107, and a flow chamber 105 defining a flow path of reagents over the microwell array 107. The reference electrode 108 may be of any suitable type or shape, including a concentric cylinder with a fluid passage or a wire inserted into a lumen of passage 111. The reagents 114 may be driven through the fluid pathways, valves, and flow cell by pumps, gas pressure, or other suitable methods, and may be discarded into the waste container 106 after exiting the flow cell and sensor array 100. The reagents 114 may, for example, contain dNTPs to be flowed through passages 130 and through the valve block 116, which may control the flow of the reagents 114 to flow chamber 105 (also referred to herein as a reaction chamber) via passage 109. The system may include a reservoir 110 for containing a wash solution that may be used to wash away dNTPs, for example, that may have previously been flowed. The microwell array 107 may include an array of defined spaces, such as microwells, for example, that is operationally associated with a sensor array so that, for example, each microwell has a sensor suitable for detecting an analyte or reaction property of interest. The defined spaces may include control/test nucleic acid samples as further described herein and/or library nucleic acid samples. The microwell array 107 may preferably be integrated with the sensor array as a single device or chip. The array controller 124 may provide bias voltages and timing and control signals to the sensor, and collect and/or process output signals. The user interface 128 may display information from the flow cell and sensor array 100 as well as instrument settings and controls, and allow a user to enter or set instrument settings and controls. The valve 112 may be shut to prevent any wash solution 110 from flowing into passage 109 as the reagents are flowing. Although the flow of wash solution may be stopped, there may still be uninterrupted fluid and electrical communication between the reference electrode 108, passage 109, and the sensor array 107. The fluidics controller 118 may be programmed to control driving forces for flowing reagents 114 and the operation of valve 112 and valve block 116 to deliver reagents to the flow cell and sensor array 100 according to a predetermined reagent flow ordering.

In this application, “defined space” generally refers to any space (which may be in one, two, or three dimensions) in which at least some of a molecule, fluid, and/or solid can be confined, retained and/or localized. The space may be a predetermined area (which may be a flat area) or volume, and may be defined, for example, by a depression or a micro-machined well in or associated with a microwell plate, microtiter plate, microplate, or a chip, or by isolated hydrophobic areas on a generally hydrophobic surface. Defined spaces may be arranged as an array, which may be a substantially planar one-dimensional or two-dimensional arrangement of elements such as sensors or wells. Defined spaces, whether arranged as an array or in some other configuration, may be in electrical communication with at least one sensor to allow detection or measurement of one or more detectable or measurable parameter or characteristics. The sensors may convert changes in the presence, concentration, or amounts of reaction by-products (or changes in ionic character of reactants) into an output signal, which may be registered electronically, for example, as a change in a voltage level or a current level which, in turn, may be processed to extract information or signal about a chemical reaction or desired association event, for example, a nucleotide incorporation event and/or a related ion concentration (e.g., a pH measurement). The sensors may include at least one ion sensitive field effect transistor (“ISFET”) or chemically sensitive field effect transistor (“chemFET”).

FIG. 3 illustrates an exemplary flow cell for nucleic acid sequencing. The flow cell 200 includes a microwell array 202, a sensor array 205, and a flow chamber 206 in which a reagent flow 208 may move across a surface of the microwell array 202, over open ends of microwells in the microwell array 202. The flow of reagents (e.g., nucleotide species) can be provided in any suitable manner, including delivery by pipettes, or through tubes or passages connected to a flow chamber. A microwell 201 in the microwell array 202 may have any suitable volume, shape, and aspect ratio. A sensor 214 in the sensor array 205 may be an ISFET or a chemFET sensor with a floating gate 218 having a sensor plate 220 separated from the microwell interior by a passivation layer 216, and may be predominantly responsive to (and generate an output signal related to) an amount of charge 224 present on the passivation layer 216 opposite of the sensor plate 220. Changes in the amount of charge 224 cause changes in the current between a source 221 and a drain 222 of the sensor 214, which may be used directly to provide a current-based output signal or indirectly with additional circuitry to provide a voltage output signal. Reactants, wash solutions, and other reagents may move into microwells primarily by diffusion 240. One or more analytical reactions to identify or determine characteristics or properties of an analyte of interest may be carried out in one or more microwells of the microwell array 202. Such reactions may generate directly or indirectly by-products that affect the amount of charge 224 adjacent to the sensor plate 220. In an embodiment, a reference electrode 204 may be fluidly connected to the flow chamber 206 via a flow passage 203. In an embodiment, the microwell array 202 and the sensor array 205 may together form an integrated unit forming a bottom wall or floor of the flow cell 200. In an embodiment, one or more copies of an analyte may be attached to a solid phase support 212, which may include microparticles, nanoparticles, beads, gels, and may be solid and porous, for example. The analyte may include one or more copies of a nucleic acid analyte, which may include a control/test nucleic acid sample as further described herein and/or a library nucleic acid sample, obtained using any suitable technique.

FIG. 4 illustrates an exemplary process for label-free, pH-based sequencing. A template 682 with sequence 685 and a primer binding site 681 are attached to a solid phase support 680. The template 682 may comprise a control/test nucleic acid sample as further described herein and/or a library nucleic acid sample. The template 682 may be attached as a clonal population to a solid support, such as a microparticle or bead, for example, and may be prepared as disclosed in Leamon et al., U.S. Pat. No. 7,323,305. In an embodiment, the template may be associated with a substrate surface or present in a liquid phase with or without being coupled to a support. A primer 684 and DNA polymerase 686 are annealed to the template 682 so that the primer's 3′ end may be extended by a polymerase and that a polymerase is bound to such primer-template duplex (or in close proximity thereof) so that binding and/or extension may take place when dNTPs are added. In step 688, dNTP (shown as dATP) is added, and the DNA polymerase 686 incorporates a nucleotide “A” (since “T” is the next nucleotide in the template 682 and is complementary to the flowed dATP nucleotide). In step 690, a wash is performed. In step 692, the next dNTP (shown as dCTP) is added, and the DNA polymerase 686 incorporates a nucleotide “C” (since “G” is the next nucleotide in the template 682). More details about pH-based nucleic acid sequencing may be found in U.S. Pat. No. 7,948,015 and U.S. Pat. Appl. Publ. Nos. 2010/0137143, 2009/0026082, and 2010/0282617.

In an embodiment, the primer-template-polymerase complex may be subjected to a series of exposures of different nucleotides in a pre-determined sequence or ordering. If one or more nucleotides are incorporated, then the signal resulting from the incorporation reaction may be detected, and after repeated cycles of nucleotide addition, primer extension, and signal acquisition, the nucleotide sequence of the template strand may be determined. The output signals measured throughout this process depend on the number of nucleotide incorporations. Specifically, in each addition step, the polymerase extends the primer by incorporating added dNTP only if the next base in the template is complementary to the added dNTP. With each incorporation, an hydrogen ion is released, and collectively a population released hydrogen ions change the local pH of the reaction chamber. The production of hydrogen ions may be monotonically related to the number of contiguous complementary bases (e.g., homopolymers) in the template. Deliveries of nucleotides to a reaction vessel or chamber may be referred to as “flows” of nucleotide triphosphates (or dNTPs). For convenience, a flow of dATP will sometimes be referred to as “a flow of A” or “an A flow,” and a sequence of flows may be represented as a sequence of letters, such as “ATGT” indicating “a flow of dATP, followed by a flow of dTTP, followed by a flow of dGTP, followed by a flow of dTTP.” The predetermined ordering may be based on a cyclical, repeating pattern consisting of consecutive repeats of a short pre-determined reagent flow ordering (e.g., consecutive repeats of pre-determined sequence of four nucleotide reagents such as, for example, “ACTG ACTG . . . ”), may be based in whole or in part on some other pattern of reagent flows (such as, e.g., any of the various reagent flow orderings discussed in Hubbell et al., U.S. Pat. Appl. Publ. No. 2012/0264621, published Oct. 18, 2012, which is incorporated by reference herein in its entirety), and may also be based on some combination thereof.

In various embodiments, output signals due to nucleotide incorporation may be processed, given knowledge of what nucleotide species were flowed and in what order to obtain such signals, to make base calls for the flows and compile consecutive base calls associated with a sample nucleic acid template into a read. A base call refers to a particular nucleotide identification (e.g., dATP (“A”), dCTP (“C”), dGTP (“G”), or dTTP (“T”)). Base calling may include performing one or more signal normalizations, signal phase and signal decay (e.g, enzyme efficiency loss) estimations, signal corrections, and model-based signal predictions, and may identify or estimate base calls for each flow for each defined space. Any suitable base calling method may be used, including as described in Davey et al., U.S. Pat. Appl. Publ. No. 2012/0109598, published on May 3, 2012, and/or Sikora et al., U.S. Pat. Appl. Publ. No. 2013/0060482, published on Mar. 7, 2013, which are all incorporated by reference herein in their entirety, recognizing of course that more accurate base callers may yield better results.

FIG. 5 illustrates an exemplary computer system. Such a computer system could be used as computing server/node/device 12 of FIG. 1. The computer system 501 includes a bus 502 or other communication mechanism for communicating information, a processor 503 coupled to the bus 502 for processing information, and a memory 505 coupled to the bus 502 for dynamically and/or statically storing information. The computer system 501 can also include one or more co-processors 504 coupled to the bus 502, such as GPUs and/or FPGAs, for performing specialized processing tasks; a display 506 coupled to the bus 502, such as a cathode ray tube (CRT) or liquid crystal display (LCD), for displaying information to a computer user; an input device 507 coupled to the bus 502, such as a keyboard including alphanumeric and other keys, for communicating information and command selections to the processor 503; a cursor control device 508 coupled to the bus 502, such as a mouse, a trackball or cursor direction keys for communicating direction information and command selections to the processor 503 and for controlling cursor movement on display 506; and one or more storage devices 509 coupled to the bus 502, such as a magnetic disk or an optical disk, for storing information and instructions. The memory 505 may include a random access memory (RAM) or other dynamic storage device and/or a read only memory (ROM) or other static storage device. Such an exemplary computer system with suitable software may be used to perform the embodiments described herein. More generally, in various embodiments, one or more features of the teachings and/or embodiments described herein may be performed or implemented using appropriately configured and/or programmed hardware and/or software elements.

Examples of hardware elements may include processors, microprocessors, input(s) and/or output(s) (I/O) device(s) (or peripherals) that are communicatively coupled via a local interface circuit, circuit elements (e.g., transistors, resistors, capacitors, inductors, and so forth), integrated circuits, application specific integrated circuits (ASIC), programmable logic devices (PLD), digital signal processors (DSP), field programmable gate array (FPGA), logic gates, registers, semiconductor device, chips, microchips, chip sets, and so forth. The local interface may include, for example, one or more buses or other wired or wireless connections, controllers, buffers (caches), drivers, repeaters and receivers, etc., to allow appropriate communications between hardware components. A processor is a hardware device for executing software, particularly software stored in memory. The processor can be any custom made or commercially available processor, a central processing unit (CPU), an auxiliary processor among several processors associated with the computer, a semiconductor based microprocessor (e.g., in the form of a microchip or chip set), a macroprocessor, or generally any device for executing software instructions. A processor can also represent a distributed processing architecture. The I/O devices can include input devices, for example, a keyboard, a mouse, a scanner, a microphone, a touch screen, an interface for various medical devices and/or laboratory instruments, a bar code reader, a stylus, a laser reader, a radio-frequency device reader, etc. Furthermore, the I/O devices also can include output devices, for example, a printer, a bar code printer, a display, etc. Finally, the I/O devices further can include devices that communicate as both inputs and outputs, for example, a modulator/demodulator (modem; for accessing another device, system, or network), a radio frequency (RF) or other transceiver, a telephonic interface, a bridge, a router, etc.

Examples of software may include software components, programs, applications, computer programs, application programs, system programs, machine programs, operating system software, middleware, firmware, software modules, routines, subroutines, functions, methods, procedures, software interfaces, application program interfaces (API), instruction sets, computing code, computer code, code segments, computer code segments, words, values, symbols, or any combination thereof. A software in memory may include one or more separate programs, which may include ordered listings of executable instructions for implementing logical functions. The software in memory may include a system for identifying data streams in accordance with the present teachings and any suitable custom made or commercially available operating system (O/S), which may control the execution of other computer programs such as the system, and provides scheduling, input-output control, file and data management, memory management, communication control, etc.

According to various embodiments, one or more features of teachings and/or embodiments described herein may be performed or implemented using an appropriately configured and/or programmed non-transitory machine-readable medium or article that may store an instruction or a set of instructions that, if executed by a machine, may cause the machine to perform a method and/or operations in accordance with the embodiments. Such a machine may include, for example, any suitable processing platform, computing platform, computing device, processing device, computing system, processing system, computer, processor, scientific or laboratory instrument, etc., and may be implemented using any suitable combination of hardware and/or software. The machine-readable medium or article may include, for example, any suitable type of memory unit, memory device, memory article, memory medium, storage device, storage article, storage medium and/or storage unit, for example, memory, removable or non-removable media, erasable or non-erasable media, writeable or re-writeable media, digital or analog media, hard disk, floppy disk, read-only memory compact disc (CD-ROM), recordable compact disc (CD-R), rewriteable compact disc (CD-RW), optical disk, magnetic media, magneto-optical media, removable memory cards or disks, various types of Digital Versatile Disc (DVD), a tape, a cassette, etc., including any medium suitable for use in a computer. Memory can include any one or a combination of volatile memory elements (e.g., random access memory (RAM, such as DRAM, SRAM, SDRAM, etc.)) and nonvolatile memory elements (e.g., ROM, EPROM, EEROM, Flash memory, hard drive, tape, CDROM, etc.). Moreover, memory can incorporate electronic, magnetic, optical, and/or other types of storage media. Memory can have a distributed, clustered, remote, or cloud architecture where various components are situated remote from one another, but are still accessed by the processor. The instructions may include any suitable type of code, such as source code, compiled code, interpreted code, executable code, static code, dynamic code, encrypted code, etc., implemented using any suitable high-level, low-level, object-oriented, visual, compiled and/or interpreted programming language.

FIG. 6 illustrates an exemplary method for nucleic acid sequencing using control sequences. In step 601, a user or component disposes a plurality of template polynucleotide strands in a plurality of defined spaces disposed on a sensor array, at least some of the template polynucleotide strands comprising a test or control sequence comprising a sequence determined by identifying, using a variant caller, loci with systematic errors present in a plurality of sequencing runs included in a training set of sequencing runs. Any suitable variant caller may be used, including the Germ-Line Variant Caller and the Torrent Variant Caller (TVC) Plug-ins for Ion Torrent™ sequencing technology, for example. In an embodiment, the variant caller may implement one or more features described in Hubbell et al., U.S. patent application Ser. No. 14/200,942, filed Mar. 7, 2014, which is incorporated by reference herein in its entirety. In step 602, a user or component exposes a plurality of the template polynucleotide strands in the defined spaces to a series of flows of nucleotide species flowed according to a predetermined ordering. Any suitable predetermined ordering may be used. For example, the predetermined ordering may be based on a cyclical, repeating pattern consisting of consecutive repeats of a short pre-determined reagent flow ordering (e.g., consecutive repeats of pre-determined sequence of four nucleotide reagents such as, for example, “ACTG ACTG . . . ”), may be based in whole or in part on some other pattern of reagent flows (such as, e.g., any of the various reagent flow orderings discussed in Hubbell et al., U.S. Pat. Appl. Publ. No. 2012/0264621, published Oct. 18, 2012, which is incorporated by reference herein in its entirety), and may also be based on some combination thereof. In step 603, a server or other computing means or resource determines sequence information for a plurality of the template polynucleotide strands in the defined spaces based on the flows of nucleotide species to generate a plurality of sequencing reads corresponding to the template polynucleotide strands. The sequence information may be determined using measured intensity values that may be related to voltage data indicative of hydrogen ion concentrations representative of a number of nucleotide incorporations responsive to each flowed nucleotide species or may include any other type of data (e.g., pyrophosphate, light, etc.) that could be representative of a number of nucleotide incorporations responsive to each flowed nucleotide species. Any suitable base calling method may be used, including as described in Davey et al., U.S. Pat. Appl. Publ. No. 2012/0109598, published on May 3, 2012, and/or Sikora et al., U.S. Pat. Appl. Publ. No. 2013/0060482, published on Mar. 7, 2013, which are all incorporated by reference herein in their entirety.

Design of Control Sequences

In various embodiments, control nucleic acid sequences (e.g., for use in sequencing-by-synthesis) may be designed based at least in part on length considerations. For example, control nucleic acid sequences may be designed to have a length in excess of 100 bases, such as at least 125 bases, at least 150 bases, at least 175 bases, at least 200 bases, at least 225 bases, at least 250 bases, or more. Such control nucleic acid sequences may be less oversensitive to errors compared to library reads than would be shorter control nucleic acid sequences (e.g., “short” sequences of 96 bases only allow one error when using a 50Q17 quality metric), and may therefore provide a more quantitative indication of run performance than shorter sequences.

In various embodiments, control nucleic acid sequences (e.g., for use in sequencing-by-synthesis) may be designed with content other than a relatively short series of homopolymers of only certain lengths. For example, control nucleic acid sequences may be designed with content that is not merely a series of homopolymers of length two, three, or four and no other length; or of homopolymers of length no more than 2; or of homopolymers of length no more than 1. Such control nucleic acid sequences with more complex content may be less sensitive to certain errors specific to particular homopolymer lengths or other phenomena such as pH drift, and may be better adapted to assess actual sequencing errors. In particular, such control nucleic acid sequences with more complex content may help provide improved determinations of general pass/fail criteria, may help support longer inserts and have similar performance/read length, and may provide sequences with single starting points that represent library read quality and that could start at multiple points of a given sequence.

In various embodiments, control nucleic acid sequences (e.g., for use in sequencing-by-synthesis) may be designed by identifying, using a variant caller, loci with systematic errors present in a plurality of sequencing runs included in a training set of sequencing runs. The control nucleic acid sequences may be generated by performing a set of sequencing runs for templates of a known library (e.g., E. coli DH10B, Lambda, synthetic sequences, etc.) under various conditions and analyzing an extent to which each of the runs is affected by one or more sequencing failure modes such as: systematic errors for high homopolymers in general, systematic errors for high homopolymers in specific contexts, and/or systematic errors for specific “difficult” sequences not involving high homopolymers. In an embodiment, control nucleic acid sequences may be generated using combinations of sequence fragments that contain multiple informative variants, such as context sequences that contain false positive variants (which may identified using variant calls made by a variant caller, as such calls would be false positives since the exact reference sequence is known). The particular combinations may be of a desired length, preferably above 100 bases. For example, the combinations may be 125, 150, 175, 200, 225, 250, or more bases in length (without adapters) comprising some segments that are known to be difficult to sequence for some known library. The combinations may be generated from identified segments in any suitable manner, including randomly in whole or in part. The size of the regions may vary and the location of the variant in the region may be at or near the center but that is not necessary. Once the regions have been selected, they may be stitched together to form a desired number of sequences of some desired length (e.g., sets of 10 regions of 20-base fragments could be stitched together to form 200-base control sequences).

FIG. 7 illustrates an exemplary method for generating control sequences. In step 701, a server or other computing means or resource identifies, using a variant caller, loci with systematic errors present in a plurality of sequencing runs included in a training set of sequencing runs obtained using sequencing-by-synthesis. In step 702, the server or other computing means or resource selects a representative set of loci, including selecting from the identified loci an approximately equal number of loci involving errors in A, T, C, and G homopolymers and selecting from the identified loci an approximately equal number of loci involving homopolymers having a length of two, three, and four.

FIG. 8 illustrates an exemplary method for generating control sequences. In step 801, a user or component obtains a set of high-throughput runs for a known reference library (e.g., E. coli DB10H). The run data may include, e.g., measured intensity values that may be related to voltage data indicative of hydrogen ion concentrations representative of a number of nucleotide incorporations or may include any other type of data (e.g., pyrophosphate, light, etc.) that could otherwise be representative of a number of nucleotide incorporations. The data may be processed and analyzed to make base calls using any suitable base calling method or approach, as discussed above. In step 802, a server or other computing means or resource identifies systematic error loci in the runs using a variant caller. Any suitable variant caller may be used, as discussed above. In step 803, the server or other computing means or resource extracts co-occurring loci. For example, loci that are present in at least a minimal number of runs (e.g., at least 3 runs) may be extracted. In some cases, that minimal threshold may be only two or may be larger (e.g., at least 4 runs, at least 5 runs, or more), and the threshold may be selected depending on the sample size. In step 804, the server or other computing means or resource discards non-informative loci. For example, loci that are present in more than a maximal number of runs (e.g., more than 20 runs) may suggest the presence of sources of error other than the ones contemplated in the present design process and may thus be discarded. In some cases, that maximal threshold may be smaller or larger than 20, and the threshold may be selected depending on the sample size. In step 805, the server or other computing means or resource selects a set of representative loci from the loci remaining after steps 803 and 804. For example, the set of representative loci may be selected to comprise an approximately equal number of loci involving errors in A, T, C, and G homopolymers and an approximately equal number of loci involving homopolymers having a length of two, three, and four. In some cases, an approximately equal number of certain homopolymer types and/or lengths may be an equal number of each type and/or length, however, depending on the data and variant calls that may not always be possible. In some cases, an approximately equal number of certain homopolymer types and/or lengths may correspond to situations where at least two of the homopolymer types and/or lengths are equal. In some cases, an approximately equal number of certain homopolymer types and/or lengths may correspond to situations where at least three of the homopolymer types and/or lengths are equal. In other cases, an approximately equal number of certain homopolymer types and/or lengths may correspond to situations where none of each homopolymer type and/or length is allowed to have a number further distant from the mean or median of the numbers of the homopolymer types and/or lengths than some pre-defined threshold. In some cases, different combinations of homopolymer types or lengths could be used (e.g., an approximately equal number of loci involving homopolymers having a length of two, four, and six; or having a length of three, four, and five; etc.) In step 806, the server or other computing means or resource extracts a context sequence from the known reference library for each of the representative loci, which may be positioned at or near the center of its corresponding context sequence although that is not necessary and other positions within the context sequence are also possible. In step 807, the extracted context sequences are combined into longer control sequences, which combination may be done in any suitable way, including by manual inspection/selection or randomly in whole or in part.

In an example, control nucleic acid sequences were generated using the following steps. In step 1, a set of 94 high-throughput E. coli DH10B runs were obtained using the Ion PGM™ system implementing Ion Torrent™ sequencing technology. In step 2, each of the 94 runs was analyzed to identify DH10B loci with systematic errors by running a variant caller on the sequencing data (as mentioned previously, since the DH10B sample has no variants relative to the reference, every called variant is in fact a false positive caused by systematic errors). Here, variant calls were obtained for the runs using the Germ-Line Variant Caller Plug-in, however, any suitable variant caller could be used also. Altogether, the runs contained 32,110 variant calls and 13,044 unique variants. FIG. 9A shows a plot of unique variants according to nucleotide (A, C, G, or T) and homopolymer length (0-mer through 12-mer). Among the unique variants, 3,464 were called in at least 3 runs and 99 were called in at least 20 runs. In step 3, each of the identified DH10B loci was analyzed to determine whether it is present in at least three of the runs (in other words, co-occurring variant locations were identified). In step 4, informative variant locations were pre-selected from the loci identified in step 3 by discarding loci with variant calls in more than 20 of the runs (if a given locus was called a variant on too many runs, that locus is likely to be systematically called differently from the reference for reasons other than the error modes of interest here). FIG. 9B shows a plot of a subset of unique variants according to nucleotide (A, C, G, or T) and homopolymer length (0-mer through 12-mer). Shown in FIG. 9B are unique variants present in at least 3 runs and at most 20 runs. In step 5, a representative set of 100 loci was selected from the loci remaining after steps 3 and 4 by selecting an approximately equal number of loci involving errors in A, T, C, and G homopolymers, and an approximately equal number of loci involving 2-mers, 3-mers, and 4-mers. Here, the loci included 25 loci for each of A, T, C, and G homopolymers, and 39 loci for each of homopolymers of length 3 and 4 with 22 loci for homopolymers of length 2. Two additional loci having consecutive homopolymers of length 5 and 2 were additionally identified. In step 6, for each locus in the representative set of loci selected in step 5, a 25-base context sequence containing that locus was extracted, with the locus being at or near the center of the context sequence. Appendix I includes a list of 102 exemplary 25-base context sequence fragments together with the position of the middle locus in the DH10B genome, the homopolymer locus (see boldface/underline) for which the context sequence was extracted, and the type and length of the homopolymer locus for which the context sequence was extracted. In step 7, 100 of the context sequences extracted in step 6 were combined in silico into groups of ten to form ten control sequences of 250 bases. Appendix II includes a list of 10 control sequences together with the homopolymer loci (see boldface/underline) for which each of the context sequences in the control sequence was extracted, and the types and lengths of the homopolymer locus for which each of the context sequences in the control sequence was extracted. For example, the first control sequence is a combination of context sequences extracted for A homopolymers of lengths 2, 3, and 4; G homopolymers of lengths 2, 3, and 4; C homopolymers of lengths 3 and 4; and T homopolymers of lengths 3 and 4. The control sequences may of course include additional homopolymers other than the ones used to extract the context sequences they comprise; only the homopolymers used to extract the context sequences are shown boldface/underline and counted in the loci types/lengths column of Appendix II.

In various examples, control sequences generated as described above may be used without further selection or they may be further tested empirically in various ways to select a smaller subset of desired control sequences for use in particular applications or in sequencing-by-synthesis generally. As part of such testing and/or sequencing, the control sequences may be synthesized and attached at one end to a sequencing adapter that may include a sequencing key identifying the sequence as a control sequence (e.g., CCAT CTCA TCCC TGCG TGTC TCCG ACAT CG, SEQ ID NO: 113), and at the other end to another adapter sequence (e.g., ATCA CCGA CTGC CCAT AGAG AGGA AAGC GGAG GCGT AGTG G, SEQ ID NO: 114). Sequence synthesis and attachment may be done using any suitable method known in the art. A series of feasibility runs may then be performed using any suitable sequencing technology, and a subset of desired control sequences may be selected based on an analysis of the runs. In some cases, some of the runs may be performed in ideal situations while others are intentionally performed under inadequate situations (e.g., by intentionally using an inadequate pH level when using Ion Torrent™ sequencing technology), and comparison of the behavior of the control sequences across ideal/inadequate situations may be used to identify control sequences that better conform or are more consistent with the underlying experimental situation. Selection of a particular subset of control sequences may be based on various accuracy criteria (e.g., mean read length, fraction of aligned reads, error(s) at particular positions, or other quality metrics), or platform-specific parameters or phenomena (e.g., pH drift), or other error sources or error-reducing goals or objectives, or some combination thereof.

According to an exemplary embodiment, there is provided a method for nucleic acid sequencing, comprising: (a) disposing a plurality of template polynucleotide strands in a plurality of defined spaces disposed on a sensor array, at least some of the template polynucleotide strands comprising a test or control sequence; (b) exposing a plurality of the template polynucleotide strands in the defined spaces to a series of flows of nucleotide species flowed according to a predetermined ordering; and (c) determining sequence information for a plurality of the template polynucleotide strands in the defined spaces based on the flows of nucleotide species to generate a plurality of sequencing reads corresponding to the template polynucleotide strands, wherein the test or control sequence comprises a sequence determined by identifying, using a variant caller, loci with systematic errors present in a plurality of sequencing runs included in a training set of sequencing runs.

In such a method, the test or control sequence may comprise a sequence further determined by finding co-occurring variant locations present in at least three sequencing runs included in a training set of sequencing runs. The test or control sequence may comprise a sequence further determined by pre-selecting informative variant locations. The test or control sequence may comprise a sequence further determined by discarding co-occurring variant locations present in more than twenty sequencing runs included in a training set of sequencing runs. The test or control sequence may comprise a sequence further determined by selecting a representative set of loci, including selecting from the set of identified loci an approximately equal number of loci involving errors in A, T, C, and G homopolymers. The test or control sequence may further comprise a sequence further determined by selecting from the set of identified loci an approximately equal number of loci involving homopolymers having a length of two, three, and four. The test or control sequence may comprise a sequence further determined by extracting a context sequence containing each locus in the representative set of loci. The test or control sequence may comprise a sequence further determined by combining in silico the extracted context sequences. The test or control sequence may comprise a sequence further determined by attaching one or more sequencing adapters to the combined sequence. The test or control sequence may comprise a sequence further determined by finding co-occurring variant locations present in at least three and no more than twenty sequencing runs included in a training set of sequencing runs. The test or control sequence may comprise a sequence further determined by finding co-occurring variant locations present in at least five and no more than fifteen sequencing runs included in a training set of sequencing runs.

According to an exemplary embodiment, there is provided a kit for nucleic acid sequencing, comprising: a plurality of test or control sequences each comprising a sequence determined by identifying, using a variant caller, loci with systematic errors present in a plurality of sequencing runs included in a training set of sequencing runs obtained using sequencing-by-synthesis, wherein the test or control sequences each comprise a sequence further determined by selecting a representative set of loci, including selecting from the identified loci an approximately equal number of loci involving errors in A, T, C, and G homopolymers and selecting from the identified loci an approximately equal number of loci involving homopolymers having a length of two, three, and four.

According to an exemplary embodiment, there is provided a system, including: a plurality of template polynucleotide strands disposed in a plurality of defined spaces disposed on a sensor array, at least some of the template polynucleotide strands comprising a test or control sequence, wherein the test or control sequence comprises a sequence determined by identifying, using a variant caller, loci with systematic errors present in a plurality of sequencing runs included in a training set of sequencing runs; a machine-readable memory; and a processor configured to execute machine-readable instructions, which, when executed by the processor, cause the system to perform a method for nucleic acid sequencing, comprising: (a) exposing a plurality of the template polynucleotide strands in the defined spaces to a series of flows of nucleotide species flowed according to a predetermined ordering; and (b) determining sequence information for a plurality of the template polynucleotide strands in the defined spaces based on the flows of nucleotide species to generate a plurality of sequencing reads corresponding to the template polynucleotide strands.

In such a system, the test or control sequence may comprise a sequence further determined by selecting a representative set of loci, including selecting from the identified loci an approximately equal number of loci involving errors in A, T, C, and G homopolymers and selecting from the identified loci an approximately equal number of loci involving homopolymers having a length of two, three, and four.

According to an exemplary embodiment, there is provided a method for designing test or control sequences, comprising: identifying, using a variant caller, loci with systematic errors present in a plurality of sequencing runs included in a training set of sequencing runs obtained using sequencing-by-synthesis; and selecting a representative set of loci, including selecting from the identified loci an approximately equal number of loci involving errors in A, T, C, and G homopolymers and selecting from the identified loci an approximately equal number of loci involving homopolymers having a length of two, three, and four.

In such a method, the test or control sequence may comprise a sequence further determined by finding co-occurring variant locations present in at least three sequencing runs included in a training set of sequencing runs. The test or control sequence may comprise a sequence further determined by pre-selecting informative variant locations. The test or control sequence may comprise a sequence further determined by discarding co-occurring variant locations present in more than twenty sequencing runs included in a training set of sequencing runs. The test or control sequence may comprise a sequence further determined by extracting a context sequence containing each locus in the representative set of loci. The test or control sequence may comprise a sequence further determined by combining in silico the extracted context sequences. The test or control sequence may comprise a sequence further determined by attaching one or more sequencing adapters to the combined sequence. The test or control sequence may comprise a sequence further determined by finding co-occurring variant locations present in at least three and no more than twenty sequencing runs included in a training set of sequencing runs. The test or control sequence may comprise a sequence further determined by finding co-occurring variant locations present in at least five and no more than fifteen sequencing runs included in a training set of sequencing runs.

Unless otherwise specifically designated herein, terms, techniques, and symbols of biochemistry, cell biology, genetics, molecular biology, nucleic acid chemistry, nucleic acid sequencing, and organic chemistry used herein follow those of standard treatises and texts in the relevant field.

Although the present description described in detail certain embodiments, other embodiments are also possible and within the scope of the present invention. For example, those skilled in the art may appreciate from the present description that the present teachings may be implemented in a variety of forms, and that the various embodiments may be implemented alone or in combination. Variations and modifications will be apparent to those skilled in the art from consideration of the specification and figures and practice of the teachings described in the specification and figures, and the claims.

APPENDIX I Position Context Sequence Fragment Type Length SEQ ID NO: 3059197 GATGCAGCACCG AA GGCTGAATATC A 2 SEQ ID NO: 1 3620936 TCTCAGGTTACG AA GGCGGTGCCAA A 2 SEQ ID NO: 2 1321265 TTGATCGACTTT AA CGTCCGTGCGG A 2 SEQ ID NO: 3 454206 AGCCCCGGCTGT AA CGTTTTGGTAT A 2 SEQ ID NO: 4 1505557 GTTTGCCGAGGC AA TATATGTCCGG A 2 SEQ ID NO: 5 3930414 CCGCCGAAGGCC AA CCCCAGTTTGA A 2 SEQ ID NO: 6 3665932 ACAGCGGCGGG AAA TTTCCCACCTG A 3 SEQ ID NO: 7 4028930 GTGGGTCAGCG AAA CGTTTCGCTGA A 3 SEQ ID NO: 8 3032774 AGCGGAACAGT AAA TTTACGGCAGA A 3 SEQ ID NO: 9 2183647 GTTATGAACCC AAA GTCAGCCGTGA A 3 SEQ ID NO: 10 2568253 GACTGCCCTTT A AA CCTGTACCCAC A 3 SEQ ID NO: 11 2903059 TACTGGCAAAT AAA GTACGTTCCAC A 3 SEQ ID NO: 12 992689 AAGAGCGTCGT AAA GTATTGCAGGT A 3 SEQ ID NO: 13 945598 TCAGGCGGCGG AAA GCGTGATTGAC A 3 SEQ ID NO: 14 1204000 CTGACGCTGCC AAA CGCCGACCGCG A 3 SEQ ID NO: 15 4284712 ATGCGCGCGTT AAA GTGCGTATCAC A 3 SEQ ID NO: 16 1221988 ATGGTTACTTT AAAA CCGGATTAAT A 4 SEQ ID NO: 17 2538868 CATCAGGCACC AAAA GAGTATGGCG A 4 SEQ ID NO: 18 3186626 ACTTCGGCACC AAAA GCATTGGCGT A 4 SEQ ID NO: 19 4566931 GCGGGAAGGGG AAAA TCCATGCTGA A 4 SEQ ID NO: 20 4235391 GTTCGTCCGTG AAAA TAAGAGTCAC A 4 SEQ ID NO: 21 887336 ATTTAAGTGAG AAAA CCGGCAGCCA A 4 SEQ ID NO: 22 3480357 CGAAATTTGAT AAAA TCCCGCTCTT A 4 SEQ ID NO: 23 2102606 GCTTGATCAGG AAAA GTTTGGTATC A 4 SEQ ID NO: 24 4286302 GTCCGGCACTG AAAA TCGTTGATGC A 4 SEQ ID NO: 25 1469524 GCTGGCGGAGCC TT CAGTCTATTTT T 2 SEQ ID NO: 26 59306 CTGGAACGCCCC TT CAACCTTAGCA T 2 SEQ ID NO: 27 3395983 AAGGCGCAGGG TTT GCAGAGCTGTT T 3 SEQ ID NO: 28 2781684 GCCACCAGCCC TTT GCTTTCCAGTG T 3 SEQ ID NO: 29 4533299 GTACCGGCAAA TTT GCCGCCGTAAG T 3 SEQ ID NO: 30 1817146 GTCGGCGCAAA TTT GCAACCAGAAG T 3 SEQ ID NO: 31 160766 GCGTGACCAAA TTT GGTGCAGCGCC T 3 SEQ ID NO: 32 3665935 GCGGCGGGAAA TTT CCCACCTGATA T 3 SEQ ID NO: 33 197121 CTCGCGGTAAA TTT ACCGAAGCACA T 3 SEQ ID NO: 34 1554427 TCCCAAACCGG TTT CGTTTAATAAT T 3 SEQ ID NO: 35 2039554 TGGCGGCGAAA TTT CGCGCCAGCGG T 3 SEQ ID NO: 36 4180498 TCCGTTACACC TTTT CCACATTCAC T 4 SEQ ID NO: 37 881464 TGTGTCAGGGC TTTT GGTTCTCCCT T 4 SEQ ID NO: 38 2659290 TCTGCAATTCA TTTT GCATATAGCC T 4 SEQ ID NO: 39 4099761 CATAACTATTG TTTT GATGAATCAG T 4 SEQ ID NO: 40 4497018 GTATCGCCAGC TTTT GCAAACGCCC T 4 SEQ ID NO: 41 2308230 ACGCTGCATCG TTTT CATCTTTAAA T 4 SEQ ID NO: 42 2425780 AGATAGCTCCC TTTT GGCATGAAGA T 4 SEQ ID NO: 43 4073210 TGTTGAACTAC TTTT CCTGATATGT T 4 SEQ ID NO: 44 3385917 AACCAGCACTC TTTT CATGGCTATC T 4 SEQ ID NO: 45 955284 ACAGGACGCCA TTTT GCCGACTCCC T 4 SEQ ID NO: 46 1018410 TCTGGCGGCAA TTTT GCTGATGGAT T 4 SEQ ID NO: 47 2212298 TCAATGGTGAC TTTT GCCGTTCCCG T 4 SEQ ID NO: 48 2380894 CTGCTGCCAGA TTTT CACCTGCTGA T 4 SEQ ID NO: 49 1765974 CTTTGACACCA TTTT CCGTAGTGAA T 4 SEQ ID NO: 50 4596308 GTTCGAGTCCGG CC TTCGGCACCAA C 2 SEQ ID NO: 51 1638520 AGGGATGGGACG CC TGTTTGCCATC C 2 SEQ ID NO: 52 821095 GATCGATCCAGG CC TAATCGATCGG C 2 SEQ ID NO: 53 3365511 ACGCTTATCAGG CC TACGCCATCTC C 2 SEQ ID NO: 54 777133 GTGGTCAGCGAG CC ACGGGTCATCA C 2 SEQ ID NO: 55 2748576 AGCAGGTGACGG CC TTCATGATCGG C 2 SEQ ID NO: 56 3298858 TTGCGGCGGTAG CC AGCTGGAAGGA C 2 SEQ ID NO: 57 4676206 CGATCGTCGCGG C C TGAATACCTGG C 2 SEQ ID NO: 58 2643681 GGAAAGCGATGG CC TACGGCGAGCG C 2 SEQ ID NO: 59 4466413 TACCTGCGCCG CCC TGGTAGACGTC C 3 SEQ ID NO: 60 3778832 AGGCGACAATG CCC TGGTCTTTCGC C 3 SEQ ID NO: 61 52406 GGGCTAAGTGG CCC TGGTGGACTCG C 3 SEQ ID NO: 62 792761 AGGCAATCGAG CCC AGATGCCGGAT C 3 SEQ ID NO: 63 4497766 CGTTGATTCTG CCC TTATTTACAAA C 3 SEQ ID NO: 64 1503858 GAATAATCCAG CCC GCCAGGCATGG C 3 SEQ ID NO: 65 2926403 CAGGCAAGCCG CCC AGGTGCTCACA C 3 SEQ ID NO: 66 1857907 GTGTTTATCAT CCC TATTGCTTTGC C 3 SEQ ID NO: 67 3638552 TATGGAAGCGG CCC AGATAAGCCAG C 3 SEQ ID NO: 68 2775787 TCAACGTGAAG CCC TGTTTAACGCT C 3 SEQ ID NO: 69 4167872 TGATATTCCTG CCCC TGATAGCGGT C 4 SEQ ID NO: 70 2160039 ATGCCGCCAGT CCCC TGATGACCCG C 4 SEQ ID NO: 71 4275966 CGGTCGTGCGA CCCC GGTAGAGCTG C 4 SEQ ID NO: 72 2878452 TGTTATATCTG CCCC GATAAAACGG C 4 SEQ ID NO: 73 3704512 AAGCCAATCAG CCCC TATCAACCGC C 4 SEQ ID NO: 74 2039072 GTCACCTGCTG CCCC ACGTGGGACA C 4 SEQ ID NO: 75 3886677 CACAGGTGATAT GG CCTTCGCCAGA G 2 SEQ ID NO: 76 4257151 AGCTACCCGATA GG CTTCCGCCATC G 2 SEQ ID NO: 77 2009720 TACGACTGCGAA GG CTTCTTCGTTG G 2 SEQ ID NO: 78 2018580 TGGGGCGGACAA GG CACTCGCGCCG G 2 SEQ ID NO: 79 3978844 CAACGGGTTATA GG CACCGCCAGGG G 2 SEQ ID NO: 80 2937614 TAGCGGTAAAC GGG CTACCGGTATC G 3 SEQ ID NO: 81 1813728 TGATTGCAACA GGG CAAATTGCGCA G 3 SEQ ID NO: 82 2716017 TGCATGAGGTC GGG TTGAATATCAA G 3 SEQ ID NO: 83 4190007 TTTCTGTTCCA GGG CTTCCGCCACC G 3 SEQ ID NO: 84 1217166 ATGACGCCAGA GGG CTGGAGATGCA G 3 SEQ ID NO: 85 906184 TCGATCCTTGA GGG ATGATTGCATT G 3 SEQ ID NO: 86 2247497 TGCGGCATACT GGG CTTCCGTATGC G 3 SEQ ID NO: 87 8186 TGATATCATCA GGG CAGACCGGTTA G 3 SEQ ID NO: 88 2795077 CACCAGAATCA GGG CAAACATATTC G 3 SEQ ID NO: 89 1807015 CCTGGTCTGGA GGG CAATACGCCCT G 3 SEQ ID NO: 90 1352099 ATCACCGAATC GGGG ACCACCGCCA G 4 SEQ ID NO: 91 1048275 GCCCATAAATT GGGG CTGATCTCCA G 4 SEQ ID NO: 92 4685037 ACAGGCTAAGA GGGG CCGGACACCC G 4 SEQ ID NO: 93 968215 CCCTGAAGGCC GGGG CAGCCCACAT G 4 SEQ ID NO: 94 193277 GATTCGGCAAA GGGG AGATACGGTT G 4 SEQ ID NO: 95 4561118 TATAGAGGATC GGGG CCACGCGCGC G 4 SEQ ID NO: 96 2141910 TCTTGCACAAA GGGG AGAAGCAATT G 4 SEQ ID NO: 97 4373401 GAACGCTATCA GGGG CAAGTTTGCA G 4 SEQ ID NO: 98 4429478 CTTCCTCGATT GGGG CTGGCGTATT G 4 SEQ ID NO: 99 1925107 GGAATCGCCCT GGGG CGGCGCACAA G 4 SEQ ID NO: 100 3147535 TATCCAAATTTTT GG CCGTTCACTG G 2 SEQ ID NO: 101 364140 TTTGCTGGAAAAA TT GCGCGCCAAA T 2 SEQ ID NO: 102

APPENDIX II Control Sequence Loci Types (Lengths) SEQ ID NO: GATGCAGCACCG AA GGCTGAATATC A (2, 3, and 4) SEQ ID NO: 103 TAGCGGTAAAC GGG CTACCGGTATC G (2, 3, and 4) TGATATTCCTG CCCC TGATAGCGGT C (3 and 4) GCCACCAGCCC TTT GCTTTCCAGTG T (3 and 4) CATCAGGCACC AAAA GAGTATGGCG TACCTGCGCCG CCC TGGTAGACGTC ACAGGCTAAGA GGGG CCGGACACCC GTTATGAACCC AAA GTCAGCCGTGA CATAACTATTG TTTT GATGAATCAG AGCTACCCGATA GG CTTCCGCCATC GCTGGCGGAGCC TT CAGTCTATTTT A (3 and 4) SEQ ID NO: 104 GGGCTAAGTGG CCC TGGTGGACTCG G (3 and 4) ATGGTTACTTT AAAA CCGGATTAAT C (2, 3, and 4) TGATTGCAACA GGG CAAATTGCGCA T (2, 3, and 4) TGTGTCAGGGC T TTT GGTTCTCCCT AGCGGAACAGT AAA TTTACGGCAGA CGGTCGTGCGA CCCC GGTAGAGCTG GTCGGCGCAAA TTT GCAACCAGAAG CCCTGAAGGCC GGGG CAGCCCACAT AGGGATGGGACG CC TGTTTGCCATC GTTCGAGTCCGG CC TTCGGCACCAA A (3 and 4) SEQ ID NO: 105 AAGGCGCAGGG TTT GCAGAGCTGTT G (3 and 4) ATCACCGAATC GGG G ACCACCGCCA C (2, 3, and 4) GTGGGTCAGCG AAA CGTTTCGCTGA T (2, 3, and 4) ATGCCGCCAGT CCCC TGATGACCCG TGCATGAGGTC GGG TTGAATATCAA TCTGCAATTCA TTTT GCATATAGCC AGGCAATCGAG CCC AGATGCCGGAT GCGGGAAGGGG AAAA TCCATGCTGA CTGGAACGCCCC TT CAACCTTAGCA CACAGGTGATAT GG CCTTCGCCAGA A (2, 3, and 4) SEQ ID NO: 106 ACAGCGGCGGG AAA TTTCCCACCTG G (2, 3, and 4) TCCGTTACACC TTTT CCACATTCAC C (3 and 4) AGGCGACAATG CCC TGGTCTTTCGC T (3 and 4) GCCCATAAATT GGGG CTGATCTCCA GTACCGGCAAA TTT GCCGCCGTAAG ACTTCGGCACC AAAA GCATTGGCGT TTTCTGTTCCA GGG CTTCCGCCACC TGTTATATCTG CCCC GATAAAACGG TCTCAGGTTACG AA GGCGGTGCCAA GACTGCCCTTT AAA CCTGTACCCAC A (2, 3, and 4) SEQ ID NO: 107 TCGATCCTTGA GGG ATGATTGCATT G (3 and 4) CAGGCAAGCCG CCC AGGTGCTCACA C (2 and 3) TCCCAAACCGG TTT CGTTTAATAAT T (3, 4, and 4) GATTCGGCAAA GGGG AGATACGGTT ACGCTGCATCG TTTT CATCTTTAAA CGAAATTTGAT AAAA TCCCGCTCTT AGCAGGTGACGG CC TTCATGATCGG TTGATCGACTTT AA CGTCCGTGCGG ACAGGACGCCA TTTT GCCGACTCCC GCGTGACCAAA TTT GGTGCAGCGCC A (2, 3, and 4) SEQ ID NO: 108 GAATAATCCAG CCC GCCAGGCATGG G (3 and 4) AAGAGCGTCGT AAA GTATTGCAGGT C (3 and 4) TGATATCATCA GGG CAGACCGGTTA T (3, 4, and 4) AAGCCAATCAG CCCC TATCAACCGC TATAGAGGATC GGGG CCACGCGCGC AGATAGCTCCC TTTT GGCATGAAGA GCTTGATCAGG AAAA GTTTGGTATC AACCAGCACTC TTTT CATGGCTATC AGCCCCGGCTGT AA CGTTTTGGTAT CGTTGATTCTG CCC TTATTTACAAA A (3 and 4) SEQ ID NO: 109 GCGGCGGGAAA TTT CCCACCTGATA G (2, 3, and 4) TGCGGCATACT GGG CTTCCGTATGC C (2, 2, and 3) TCAGGCGGCGG AAA GCGTGATTGAC T (3 and 4) GTATCGCCAGC TTTT GCAAACGCCC ATTTAAGTGAG AAAA CCGGCAGCCA GTGGTCAGCGAG CC ACGGGTCATCA GAACGCTATCA GGGG CAAGTTTGCA GATCGATCCAGG CC TAATCGATCGG TGGGGCGGACAA GG CACTCGCGCCG ATGACGCCAGA GGG CTGGAGATGCA A (3 and 4) SEQ ID NO: 110 TACTGGCAAAT AAA GTACGTTCCAC G (2, 3, and 4) CTCGCGGTAAA TTT ACCGAAGCACA C (2, 3, and 4) GTGTTTATCAT CCC TATTGCTTTGC T (3 and 4) GTTCGTCCGTG AAAA TAAGAGTCAC GTCACCTGCTG CCCC ACGTGGGACA TCTTGCACAAA GGGG AGAAGCAATT TGTTGAACTAC TTTT CCTGATATGT TACGACTGCGAA GG CTTCTTCGTTG ACGCTTATCAGG CC TACGCCATCTC GTCCGGCACTG AAAA TCGTTGATGC A (2 and 4) SEQ ID NO: 111 CTTTGACACCA TTTT CCGTAGTGAA G (2, 2, and 3) TTGCGGCGGTAG CC AGCTGGAAGGA C (2 and 3) CAACGGGTTATA GG CACCGCCAGGG T (4, 4, and 4) TATCCAAATTTTT GG CCGTTCACTG GTTTGCCGAGGC AA TATATGTCCGG TCTGGCGGCAA TTTT GCTGATGGAT TCAACGTGAAG CCC TGTTTAACGCT CACCAGAATCA GGG CAAACATATTC CTGCTGCCAGA TTTT CACCTGCTGA TATGGAAGCGG CCC AGATAAGCCAG A (3 and 3) SEQ ID NO: 112 CCTGGTCTGGA GGG CAATACGCCCT G (3, 4, and 4) CTGACGCTGCC AAA CGCCGACCGCG C (2 and 3) TGGCGGCGAAA TTT CGCGCCAGCGG T (2, 3, and 4) TTTGCTGGAAAAA TT GCGCGCCAAA CGATCGTCGCGG CC TGAATACCTGG CTTCCTCGATT GGGG CTGGCGTATT ATGCGCGCGTT AAA GTGCGTATCAC TCAATGGTGAC TTTT GCCGTTCCCG GGAATCGCCCT GGGG CGGCGCACAA 

The invention claimed is:
 1. A method for nucleic acid sequencing, comprising: (a) disposing a plurality of template polynucleotide strands in a plurality of defined spaces disposed on a sensor array, at least some of the template polynucleotide strands comprising a test or control sequence, wherein the test or control sequence is generated by combining sequences corresponding to at least two loci that meet a systematic error criteria, and the at least two loci are determined to meet the systematic error criteria based on a training set of sequencing runs in which each of the at least two loci is determined to cause a plurality of sequencing errors; (b) exposing a plurality of the template polynucleotide strands in the defined spaces to a series of flows of nucleotide species flowed according to a predetermined ordering; and (c) determining sequence information for a plurality of the template polynucleotide strands in the defined spaces based on the flows of nucleotide species to generate a plurality of sequencing reads corresponding to the template polynucleotide strands.
 2. The method of claim 1, wherein the test or control sequence comprises a sequence determined by identifying co-occurring variant locations present in at least three sequencing runs included in the training set of sequencing runs.
 3. The method of claim 1, wherein the test or control sequence comprises a sequence determined by pre-selecting informative variant locations.
 4. The method of claim 1, wherein the test or control sequence comprises a sequence determined by discarding co-occurring variant locations present in more than twenty sequencing runs included in a training set of sequencing runs.
 5. The method of claim 1, wherein the test or control sequence comprises a sequence determined by selecting a representative set of loci, including selecting from the identified loci an approximately equal number of loci involving errors in A, T, C, and G homopolymers, the representative set comprising the at least two loci.
 6. The method of claim 5, wherein the test or control sequence comprises a sequence determined by selecting from the representative set of loci an approximately equal number of loci involving homopolymers having a length of two, three, and four, wherein the at least two loci are selected from the representative set.
 7. The method of claim 6, wherein the test or control sequence comprises a sequence determined by extracting a context sequence containing each selected locus.
 8. The method of claim 7, wherein the test or control sequence comprises a sequence determined by combining in silico the extracted context sequences.
 9. The method of claim 8, wherein the test or control sequence comprises a sequence determined by attaching one or more sequencing adapters to the combined sequence.
 10. The method of claim 1, wherein the test or control sequence comprises at least 125 bases, 150 bases, 175 bases, 200 bases, 225 bases, or 250 bases.
 11. The method of claim 10, wherein the test or control sequence comprises a set of 10 regions each of at least 20 bases in size, the sequences corresponding to the at least two loci that meet the systematic error criteria each comprising one of the regions.
 12. The method of claim 1, wherein the at least two loci are determined to meet the systematic error criteria when the loci comprise co-occurring variant locations present in at least three sequencing runs included in the training set of sequencing runs.
 13. The method of claim 1, wherein the at least two loci are determined to meet the systematic error criteria when the loci comprise co-occurring variant locations that are not present in more than twenty sequencing runs included in a training set of sequencing runs.
 14. The method of claim 1, wherein the at least two loci are determined to meet the systematic error criteria when the loci comprise approximately equal number of sequencing errors in A, T, C, and G homopolymers.
 15. The method of claim 14, wherein the at least two loci are determined to meet the systematic error criteria when the loci comprise an approximately equal number homopolymers having a length of two, three, and four.
 16. The method of claim 1, wherein the test or control sequence comprises extracted context sequences of the at least two loci determined to meet the systematic error criteria combined in silico.
 17. The method of claim 16, wherein the at least two loci are determined by performing the training set of sequencing runs for a genetic template with a known genomic library.
 18. The method of claim 17, wherein the at least two loci are variants of the genetic template with the known genomic library and the context sequences are extracted from a known library sequence corresponding to each locus.
 19. A system, including: a plurality of template polynucleotide strands disposed in a plurality of defined spaces disposed on a sensor array, at least some of the template polynucleotide strands comprising a test or control sequence, wherein the test or control sequence is generated by combining sequences corresponding to at least two loci that meet a systematic error criteria, and the at least two loci are determined to meet the systematic error criteria based on a training set of sequencing runs in which each of the at least two loci is determined to cause a plurality of sequencing errors; a machine-readable memory; and a processor configured to execute machine-readable instructions, which, when executed by the processor, cause the system to perform a method for nucleic acid sequencing, comprising: (a) exposing a plurality of the template polynucleotide strands in the defined spaces to a series of flows of nucleotide species flowed according to a predetermined ordering; and (b) determining sequence information for a plurality of the template polynucleotide strands in the defined spaces based on the flows of nucleotide species to generate a plurality of sequencing reads corresponding to the template polynucleotide strands.
 20. The system of claim 19, wherein the test or control sequence comprises a sequence determined by selecting a representative set of loci, including selecting from the identified loci an approximately equal number of loci involving errors in A, T, C, and G homopolymers and selecting from the identified loci an approximately equal number of loci involving homopolymers having a length of two, three, and four, the representative set of loci including the at least two loci determined to meet the systematic error criteria. 